Manufacturing an electrode array for a stimulating medical device

ABSTRACT

A method of forming an electrode array is disclosed, the method comprising: forming an elongate comb structure comprising a plurality of longitudinally-spaced electrode contacts extending from and supported by a spine; electrically connecting each of a plurality of electrically conductive pathways to a respective one of the plurality of electrode contacts; placing the conductive pathways adjacent the contacts; placing silicone over the conductive pathways and contacts; curing the silicone so as to substantially retain the longitudinal spacing between neighboring contacts; and severing the spine from the plurality of electrode contacts.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a Continuation application of U.S. patentapplication Ser. No. 14/622,130, filed Feb. 13, 2015, which is aDivisional application of U.S. patent application Ser. No. 12/743,369,filed Aug. 26, 2010, which is a National Stage of InternationalApplication No. PCT/US2008/083794, filed Nov. 17, 2008, which is aContinuation-in-part of U.S. patent application Ser. No. 10/581,090,filed Feb. 16, 2007, which is a National Stage of InternationalApplication No. PCT/AU2004/01726, filed Dec. 8, 2004. Additionally, thisapplication claims foreign priority benefit of Australia Application No.2007906282, filed Nov. 16, 2007, Australia Application No. 2004905355,filed Sep. 16, 2004, and Australia Application No. 2003906787, filedDec. 8, 2003. Each of these applications is hereby incorporated byreference herein in their entirety.

BACKGROUND

The present invention relates generally to implantable electrodes, andmore particularly, to an electrode array for use in medical implants.

RELATED ART

There are a variety of medical implants that deliver electricalstimulation to a patient or recipient (“recipient” herein) for a varietyof therapeutic benefits. For example, the hair cells of the cochlea of anormal healthy ear convert acoustic signals into nerve impulses. Peoplewho are profoundly deaf due to the absence or destruction of cochleahair cells are unable to derive suitable benefit from conventionalhearing aid devices. A type of prosthetic hearing implant systemcommonly referred to as a cochlear implant has been developed to providesuch persons with the ability to perceive sound. A cochlear implantbypasses the hair cells in the cochlea to directly deliver electricalstimulation to auditory nerve fibers, thereby allowing the brain toperceive a hearing sensation resembling the natural hearing sensation.

The electrodes utilized in stimulating medical implants vary accordingto the device and tissue which is to be stimulated. For example, thecochlea is tonotopically mapped and partitioned into regions, with eachregion being responsive to stimulus signals in a particular frequencyrange. To accommodate this property of the cochlea, cochlear implantstypically include an array of electrodes each constructed and arrangedto deliver an appropriate stimulating signal to a particular region ofthe cochlea.

SUMMARY

In accordance with one embodiment of the present invention, a method offorming an electrode array is disclosed, the method comprising: formingan elongate comb structure comprising a plurality oflongitudinally-spaced electrode contacts extending from and supported bya spine; electrically connecting a plurality of electrically conductivepathways to the plurality of electrode contacts; constraining theplurality of contacts to substantially retain the longitudinal spacingbetween neighboring contacts; and severing the electrode contacts fromthe spine.

In accordance with another embodiment of the present invention, a methodof forming an electrode array is disclosed, the method comprising:forming an elongate comb structure comprising a plurality oflongitudinally-spaced electrode contacts extending from and supported bya spine; electrically connecting each of a plurality of electricallyconductive pathways to a respective one of the plurality of electrodecontacts; placing the conductive pathways adjacent the contacts; placingsilicone over the conductive pathways and contacts; curing the siliconeso as to substantially retain the longitudinal spacing betweenneighboring contacts; and severing the spine from the plurality ofelectrode contacts.

BRIEF DESCRIPTION OF THE DRAWINGS

Aspects and embodiments of the present invention are described hereinwith reference to the accompanying drawings, in which:

FIG. 1A is a perspective view of an exemplary medical device, a cochlearimplant, having an electrode assembly which may be advantageouslymanufactured using embodiments of the present invention;

FIG. 1B is a side view of the implantable components of the cochlearimplant illustrated in FIG. 1A;

FIG. 2 is a side view of an embodiment of the electrode arrayillustrated in FIGS. 1A and 1B in a curled orientation;

FIG. 3 is a schematic view of the electrode array of FIG. 2 in situ in acochlea;

FIG. 4 is a perspective view of intermediate manufacturing product, acomb, which may be used during manufacture of an electrode array inaccordance with embodiments of the present invention;

FIG. 5 is a perspective magnified view of a portion of the combillustrated in FIG. 4;

FIG. 6 is a side view of an individual electrode contact on the combillustrated in FIG. 5, in accordance with embodiments of the presentinvention;

FIG. 7 is a side view of the electrode contact illustrated in FIG. 6with conductive pathways in the form of wires shown positioned in thetrough of the contact;

FIG. 8 is a top view of an intermediate manufactured product showing acut line for removing the spine from the teeth of the comb, inaccordance with embodiments of the present invention;

FIG. 9 is a flowchart of a method of making the comb of FIG. 4, inaccordance with embodiments of the present invention;

FIG. 10 is a flowchart of a method of making an electrode assembly shownin FIGS. 1-3, using the comb of FIG. 4, in accordance with embodimentsof the present invention;

FIG. 11 shows an alternative electrode contact configuration with aV-notch;

FIG. 12 shows an alternative configuration for the comb illustrated inFIGS. 4 and 5;

FIG. 13 shows an alternative configuration for the comb illustrated inFIGS. 4 and 5;

FIG. 14 shows an alternative configuration for the comb illustrated inFIGS. 4 and 5;

FIG. 15 shows an alternative configuration for the comb illustrated inFIGS. 4 and 5; and

FIG. 16 shows an arrangement of two combs on sheet of electricallyconductive material, in accordance with embodiments of the presentinvention.

DETAILED DESCRIPTION

Embodiments of the present invention are described herein primarily inconnection with one type of hearing prosthesis, namely a cochlearimplant. Cochlear implants generally refer to hearing prostheses thatdeliver electrical stimulation to the cochlea of a recipient. As usedherein, the term “cochlear implant” also include hearing prostheses thatdeliver electrical stimulation in combination with other types ofstimulation, such as acoustic or mechanical stimulation. It would beappreciated that embodiments of the present invention may be implementedin any cochlear implant or other hearing prosthesis now known or laterdeveloped, including auditory brain stimulators, or implantable hearingprostheses that also acoustically or mechanically stimulate componentsof the recipient's middle or inner ear.

FIG. 1A is a perspective view of an exemplary medical device having anelectrode carrier member manufactured in accordance with the teachingsof the present invention. Specifically, FIG. 1A is perspective view of acochlear implant 100 implanted in a recipient having an outer ear 101, amiddle ear 105 and an inner ear 107. Components of outer ear 101, middleear 105 and inner ear 107 are described below, followed by a descriptionof cochlear implant 100.

In a fully functional ear, outer ear 101 comprises an auricle 110 and anear canal 102. An acoustic pressure or sound wave 103 is collected byauricle 110 and channeled into and through ear canal 102. Disposedacross the distal end of ear cannel 102 is a tympanic membrane 104 whichvibrates in response to sound wave 103. This vibration is coupled tooval window or fenestra ovalis 112 through three bones of middle ear105, collectively referred to as the ossicles 106 and comprising themalleus 108, the incus 109 and the stapes 111. Bones 108, 109 and 111 ofmiddle ear 105 serve to filter and amplify sound wave 103, causing ovalwindow 112 to articulate, or vibrate in response to vibration oftympanic membrane 104. This vibration sets up waves of fluid motion ofthe perilymph within cochlea 140. Such fluid motion, in turn, activatestiny hair cells (not shown) inside of cochlea 140. Activation of thehair cells causes appropriate nerve impulses to be generated andtransferred through the spiral ganglion cells (not shown) and auditorynerve 114 to the brain (also not shown) where they are perceived assound.

Cochlear implant 100 comprises an external component 142 which isdirectly or indirectly attached to the body of the recipient, and aninternal component 144 which is temporarily or permanently implanted inthe recipient. External component 142 typically comprises one or moresound input elements, such as microphone 124, for detecting sound, asound processing unit 126, a power source (not shown), and an externaltransmitter unit 128. External transmitter unit 128 comprises anexternal coil 130 and, preferably, a magnet (not shown) fixed relativeto external coil 130. Sound processing unit 126 processes the output ofmicrophone 124 that is positioned, in the depicted embodiment, byauricle 110 of the recipient. Sound processing unit 126 generatesencoded signals, sometimes referred to herein as encoded data signals,which are provided to external transmitter unit 128 via a cable (notshown).

Internal component 144 comprises an internal receiver unit 132, astimulator unit 120, and an elongate electrode assembly 118, alsoreferred to as a lead. Internal receiver unit 132 comprises an internalcoil 136, and preferably, a magnet (also not shown) fixed relative tothe internal coil. Internal receiver unit 132 and stimulator unit 120are hermetically sealed within a biocompatible housing, and aresometimes collectively referred to as a stimulator/receiver unit. Theinternal coil receives power and stimulation data from external coil130, as noted above. Elongate electrode assembly 118 has a proximal endconnected to stimulator unit 120, and a distal end implanted in cochlea140. Electrode assembly 118 extends from stimulator unit 120 to cochlea140 through mastoid bone 119. As described below, electrode assembly 118is implanted in cochlea 140. In some embodiments electrode assembly 118may be implanted at least in basal region 116, and sometimes further.For example, electrode assembly 118 may extend towards apical region, orapex, 134 of cochlea 140. In certain circumstances, electrode assembly118 may be inserted into cochlea 140 via a cochleostomy 122. In othercircumstances, a cochleostomy may be formed through round window 121,oval window 112, the promontory 123 or through an apical turn 147 ofcochlea 140.

Electrode assembly 118 comprises a plurality of longitudinally alignedand distally extending electrodes 148 disposed along a length thereof.In most practical applications, electrodes 148 are integrated intoelectrode assembly 118. As such, electrodes 148 are referred to hereinas being disposed in electrode assembly 118. Stimulator unit 120generates stimulation signals which are applied by electrodes 148 tocochlea 140, thereby stimulating auditory nerve 114.

In cochlear implant 100, external coil 130 transmits electrical signals(i.e., power and stimulation data) to internal coil 136 via a radiofrequency (RF) link. Internal coil 136 is typically a wire antenna coilcomprised of multiple turns of electrically insulated single-strand ormulti-strand platinum or gold wire. The electrical insulation ofinternal coil 136 is provided by a flexible silicone molding. In use,implantable receiver unit 132 may be positioned in a recess of thetemporal bone adjacent auricle 110 of the recipient.

While various aspects of the present invention are described withreference to a cochlear implant, it will be understood that variousaspects of the present invention are equally applicable to otherstimulating medical devices having an array of electrical simulatingelectrodes such as auditory brain implant (ABI), functional electricalstimulation (FES), spinal cord stimulation (SCS), penetrating ABIelectrodes (PABI), and so on. Further, it should be appreciated that thepresent invention is applicable to stimulating medical devices havingelectrical stimulating electrodes of all typessuch as straightelectrodes, peri-modiolar electrodes and short/basilar electrodes.

Throughout this description, the term “electrode array” means acollection of two or more electrodes, sometimes referred to as electrodecontacts or simply contacts herein. The term “electrode array” alsorefers to or includes the portion of the carrier member in which theelectrodes are disposed. It should be appreciated that in the literatureand prior art the term “electrode array” refers to both, the electrodesas well as the combination of electrodes and the carrier member in whichthe electrodes are disposed.

FIG. 1B is a side view of an internal component 144 of a conventionalcochlear implant. Internal component 144 comprises a receiver/stimulator180 and an electrode assembly or lead 118. Electrode assembly 118includes a helix region 182, a transition region 184, a proximal region186, and an intra-cochlear region 188. Proximal region 186 andintra-cochlear region 188 form an electrode array 190. Electrode array190, and in particular, intra-cochlear region 188 of electrode array190, supports a plurality of electrode contacts 149. These electrodecontacts 148 are each connected to a respective conductive pathway, suchas wires, PCB traces, etc. (not shown) which are connected through lead118 to receiver/stimulator 180, through which respective stimulatingelectrical signals for each electrode contact 148 travel.

FIG. 2 is a side view of electrode array 190 in a curled orientation, asit would be when in situ in a patient's cochlea, with electrode contacts148 located on the inside of the curve. FIG. 3 shows the electrode arrayof FIG. 2 in situ in a patient's cochlea 140. In this exemplaryapplication, electrode contacts 148 are shown in electrical contact withthe tissue to be stimulated, as will be understood by those skilled inthe art.

FIG. 4 is a perspective view of an intermediate product 400 made duringmanufacture of an electrode array 190 in accordance with embodiments ofthe present invention. As shown in FIG. 4, electrode contacts 148 areformed from the unitary piece 400 of electrically conductive material,referred to herein as a “comb” 400. Comb 400 includes a number of teeth404 extending from and supported by a spine 402. In the example shown,there are twenty-two teeth/electrode contacts 404 extending from anelongate spine 402. In practice, there may be any number of electrodecontacts, ranging from 2 to 256 electrode contacts, or more. This may,for example, include 3, 4, 5, 6, 7, 8, 9, 10, 10-20, 20-30, 30-50,50-100, 100-150, 150-200, 200-256, 256-300 electrode contacts, etc.

Electrode contacts 148 are preferably made from platinum, but any othersuitable material such as iridium, a platinum/iridium alloy, or otherplatinum or iridium alloy may be used, as will be understood by one ofordinary skill in the art.

For certain applications, electrode contacts 148 are preferably formedin a U-shape, as shown in FIGS. 5 and 6. FIG. 5 is a magnified view of aportion of comb 400; FIG. 6 is a side view of an individual electrodecontact 148 on comb 400. At this stage of manufacture, electrodes 148are in the form of teeth of comb 400. As shown in FIG. 6, teeth 404 havea relatively large exposed surface area. Electrode array 190 isparticularly adapted to bend and flex in one direction, making itwell-suited to inserting into a curved body cavity, such as cochlea 50.

Preferably, the width of each tooth 404 of comb 400 is 0.3 mm and thegap between them is approximately 0.3 mm. The total length of such acomb is approximately 13 mm, based upon the preferred number of teeth404. Of course, these dimensions may be varied as required by theparticular design and application.

FIG. 5 also shows conductive pathways (in this example wires) 502connected to respective teeth 404. The method of connection may be donein any suitable manner such as welding, as will be described in moredetail below. FIG. 7 is a side view of a tooth/contact 148 showing thecollection of conductive wires 502 being supported in the trough of oneof the U-shaped teeth 404. Once wires 502 have been connected toelectrode contacts 148, electrode contacts 148 are cut off or otherwisesevered from spine 402. The cut point is preferably just below spine 402so that contacts 148 are of a substantially rectangular shape, as shownin FIG. 8.

Spine 402 of comb 400 serves a dual function. Firstly, spine 402connects electrode contacts 148 so that the contacts are in one pieceand thus in a fixed location relative to each other. Secondly, spine 402provides a secure holding point to secure comb 400 to the welding jig(not shown), thus holding electrode contacts 3 during subsequentprocessing operations.

A method of forming the comb 400 is described below with reference toFIG. 9. At step 902, a platinum sheet having a thickness of, forexample, 50 um, is worked (in this example, punched) to provide theshape of comb 400 as shown in FIG. 8. Of course other methods may beused to form comb 400, such as EDM to micromachine the combs. It isenvisaged that in certain applications smaller contacts will be desiredand once the limitations of punching electrodes has been reached theycould be cut out using a laser and subsequently formed using the methodsdescribed above or out using a laser and formed using laser ablation.

Rotary knife tooling could also be used to cut a platinum sheet, orother materials, into electrode contacts with a spine or with anadhesive backing where the rotary blades cut through the first layerleaving the spine intact, and following forming, welding, molding etc.the second layer can be peeled off. Various other techniques forpunching, cutting, and otherwise working the sheet are also described inInternational Patent Publication No. WO 02/089907.

In step 904, the planar comb is formed into its 3-dimensional shape asshown in FIGS. 4 and 5 by forming a U-shape in teeth 804. In step 906,the shaped comb is washed in preparation for welding. It is possible toform a plurality of combs from a single sheet of material. For example,about 25 combs can be formed quasi-simultaneously from a platinum strip500 mm in length via a pneumatic press.

The method of forming electrodes 148 from the formed comb 400 isdescribed with reference to FIG. 10. At step 1002, the finishedthree-dimensional comb 400 is placed into a welding jig (not shown)ready for wires 32 to be joined to the comb. The comb 400 is secured bybeing held along the length of the spine 31, thereby providing a securehold.

At step 1004, a wire 32 is welded to the most proximal electrode contact148. At step 1006, an amount (for example a droplet) of silicone isplaced in the trough of the electrode contact 148. In step 1008, asecond wire 502 is welded to the second most proximal electrode contact148. At step 1010, the wire from the second contact is bedded down intothe silicone droplet in the trough of the first electrode. In step 1012,a droplet of silicone is placed in the trough of the second electrodecontact. In step 1014, steps 1002 through 1012 are repeated until allwires 502 have been connected to their respective electrode contacts148. As one of ordinary skill in the art would appreciate, the sequenceof placing the wires and silicone may be different in alternativeembodiments of the present invention. Similarly, it should beappreciated that each wire, or all wires, may be placed in the electrodetroughs in a single operation followed by the application of silicone tonone, some or all of such troughs.

After all wires have been connected, a production stylet (for example, aPTFE coated wire) is suspended above or otherwise placed on top of thewires in step 1016. This stylet is removed later and forms the lumen oflead. In step 608, silicone is placed above each contact over theproduction stylet, to form a sub-assembly, and the silicone is cured inan oven in step 1020. At this point in the process the electrodecontacts 148 are substantially constrained in a relative longitudinalposition thereby substantially retaining the longitudinal spacingbetween neighboring contacts.

In step 1022, the sub-assembly is removed from the welding jig. In step1024, spine 402 is then severed such as by cutting from comb 400 toleave the individual electrode contacts 148. In alternative embodiments,a V-notch 1102 is formed in teeth 148 to facilitate separation of theteeth from spine 402 simply by “snapping off” the teeth, as shown inFIG. 11. Alternatively, the separation of teeth 804 from spine 402 maybe facilitated by forming a part of the teeth 804 with a narrower partsuch as shown in FIG. 12. This provides an alternative “snapping”option.

It is also possible to change the order of some of the steps above. Forexample, the step 501 of forming the comb into a 3-dimensional shape maybe performed after the steps of welding the conductive wires 32 intoplace. Performing the steps in other sequences is also contemplated. Itis also possible to connect 2 or more wires to one or more electrodes.This may provide an advantage of redundancy and may increase therobustness of the resulting lead 20.

The process continues as is known in the art. In particular, one methodof molding of electrode array is as described in U.S. Pat. No.6,421,569, the disclosure of which is incorporated by reference.

The sub-assembly is preferably carefully curved to match the shape of acurved molding die (not shown). The assembly is then placed in thecurved molding die with the contacts being located closer to the medialside (inside of the curve). The space in the die is packed with siliconematerial. A matching die cover is placed over the assembly and presseddown. The die is then placed in an oven to cure the silicone. The die isthen open to allow the resulting electrode array to be removed from thedie.

The electrode array described above forms the distal end of leadassembly 20 that is adapted to be connected to implantablereceiver/stimulator 10 (FIG. 1). Receiver/stimulator 10 is typicallyhoused within a metallic case. In one application, receiver/stimulator10 has an array of feed through terminals corresponding to its multiplechannels.

The electrode array facilitates the use of non-flat surface finishes.For example, dimpled, corrugated, pitted or irregular geometric shapesmay be provided on the surface of electrode contacts 30. These variedsurface finishes may be achieved by stamping a pattern finish in thepunching and pre-forming operation. Alternatively, the contact areas maybe roughened by controlled sandblasting of the array before or aftermolding. Surface modification may also be achieved using laser ablationvia the direct write method or using a mask at almost any stage duringthe manufacture of the electrode. A non-flat surface area may have theadvantage of increasing the effective size of the electrode contactwithout requiring a larger electrode contact. This allows smallerelectrode contacts with equivalent surface areas to be utilized. Variousmethods of creating such surface finishes are described in for example,U.S. Pat. No. 4,602,637 and PCT Application No. PCT/US2006/036966(WO2007/050212)

Alternatively, the electrode contacts may be substantially planar ratherthan U-shaped as described above. In this embodiment, comb 400 may bepunched rather than formed. Such embodiments provide for a relativelysimpler manufacturing processing. In alternative embodiments, electrodecontacts 30 have a shape other than rectangular, such as square,circular, triangular or oval.

In yet another alternative, the various aspects of the present inventionmay be used to provide electrode arrays with a variable pitch. Suchconstructions are disclosed in U.S. Pat. No. 7,184,843. For example,comb 400 can be formed with teeth 404 having a variable spacing, withthe distal electrode contacts lying closer together than the proximalones. Other variations on the spacing between electrode contacts mayalso be utilized.

In yet another alternative, a stepped sheet of a varying thickness canbe used to create comb 400 with spine 402, as shown in FIG. 13. This hasthe advantage of increasing the torsional stability of teeth/electrodecontacts 404 while maintaining a relatively consistent contactthickness.

In yet another alternative, spine 402 runs between electrode contacts404, as shown in FIG. 14.

In alternative embodiments, comb 300 may be formed to have asubstantially cylindrical shape as shown in FIG. 15. In one suchembodiment, electrode contacts 404 are circular with both ends connectedto spine 402. In manufacturing such a structure, teeth 404 may be rolledinto shape, or alternatively, they may be formed by etching the shapefrom a continuous platinum tube.

In yet another embodiment, two separate (not connected) spines 31, 31′hold two sets of respective electrode contacts 30, 30′ as shown in FIG.16.

In yet another alternative, two or more arrays may be formed andlaminated together to form a single tissue stimulating electrodeassembly. For example, such an assembly might be formed from a firstlamination having seven electrodes, a second lamination having eightelectrodes, and a third lamination having eight electrodes, to form anelectrode assembly having 23 electrodes. In the case of a cochlearelectrode array, the formed array may have 22 intracochlear electrodesand one extracochlear electrode. Such a lamination process wouldpreferably result in a linear array of the 22 electrodes. Othercombinations of layers, and other quantities of electrodes in eachlayer, may be utilized to form arrays of different lengths.

In the descriptions above, the electrically conductive pathways may beprovided by any suitable means including wires, conductive deposits,conductive tracks, and the like.

The above and other embodiments of forming electrode arrays, and theelectrode arrays themselves, may provide one or more advantages overconventional methods. Such advantages may include, and are not limitedto the following: they may be manufactured using easy, low costtechnology; they have lower parts count (for 22 electrode contacts, theparts count has reduced by 21); they have higher a Manufacturing YieldRate (fewer problems during holding contacts during at least welding);and they enable greater accuracy and consistency with contact placement.

While various embodiments of the present invention have been describedabove, it should be understood that they have been presented by way ofexample only, and not limitation. It will be apparent to persons skilledin the relevant art that various changes in form and detail can be madetherein without departing from the spirit and scope of the invention.Thus, the breadth and scope of the present invention should not belimited by any of the above-described exemplary embodiments, but shouldbe defined only in accordance with the following claims and theirequivalents.

What is claimed is:
 1. An apparatus, comprising: a spine segment; and atoothed segment, wherein the spine segment and toothed segment are partof a monolithic component, and the monolithic component is anelectrically conductive biocompatible material.
 2. The apparatus ofclaim 1, wherein: the toothed segment comprises a plurality of teethextending away from the spine segment and the spine segment holds theteeth of the plurality of teeth relative to one another.
 3. Theapparatus of claim 1, wherein: there are at least 5 teeth making up thetoothed segment.
 4. The apparatus of claim 3, wherein: the length of thespine segment is at least 260 times a thickness of the spine segment. 5.The apparatus of claim 3, wherein: the length of the spine segment is atleast two (2) orders of magnitude greater than a thickness of the spinesegment.
 6. The apparatus of claim 3, wherein: the toothed segment has across-section that has a U-shaped portion, which cross-section lies on aplane normal to a longitudinal axis of the spine segment.
 7. Theapparatus of claim 3, wherein: the toothed segment includes a pluralityof teeth, respective teeth of the plurality of teeth have a width thatis greater than a thickness, the width being measured in a direction ofa longitudinal axis of the spine segment, and the thickness being normalto the width and the width is less than respective heights of therespective teeth.
 8. The apparatus of claim 3, wherein: the toothedsegment includes a plurality of teeth, all teeth of the apparatus arearrayed in a single line along a length of extension of the spinesegment.
 9. The apparatus of claim 3, wherein: the spine segment andtoothed segment form an elongate comb.
 10. The apparatus of claim 1,further comprising: a wired segment, wherein the wired segment is notmonolithic with the monolithic component.
 11. The apparatus of claim 1,further comprising: a wired portion, wherein the wired portion comprisesa plurality of wires, the wires of the plurality of wires beingrespectively connected to respective teeth of the toothed section. 12.The apparatus of claim 11, further comprising: a silicone body in whichrespective first portions of respective teeth of the toothed section arelocated, wherein the spine segment is outside of the silicone body. 13.The apparatus of claim 12, wherein: the silicone body, the monolithiccomponent and the wired portion form an embryonic electrode array of acochlear implant.
 14. The apparatus of claim 12, wherein: the apparatusis part of an embryonic electrode assembly that consists of the siliconebody, the monolithic component and the wired portion.
 15. The apparatusof claim 11, wherein: the teeth of the toothed portion are concavelybent and the spine is flat.
 16. The apparatus of claim 15, wherein: thewires are located on the concave sides of the teeth.
 17. The apparatusof claim 1, wherein: the spine segment and the toothed segmentcollectively are in a shape of a rake.
 18. The apparatus of claim 1,wherein: the spine segment and the toothed segment collectively form acomb.
 19. The apparatus of claim 1, wherein: in a direction of alongitudinal axis of the monolithic component, the distance betweenrespective teeth of the toothed segment is approximately 0.3 mm and awidth of the teeth is at least about the same.
 20. An assembly,comprising: a spine segment; a toothed segment; a wired portion, whereinthe wired portion comprises a plurality of wires, the wires of theplurality of wires being respectively connected to respective teeth ofthe toothed section; and a silicone body in which respective firstportions of respective teeth of the toothed section are located, whereinthe spine segment is outside of the silicone body, wherein the spinesegment and toothed segment are part of a monolithic component, themonolithic component is an electrically conductive biocompatiblematerial, and the assembly consists of the silicone body, the monolithiccomponent and the wired portion.